Dejerine–Sottas disease
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Dejerine–Sottas disease
Summary
Dejerine–Sottas disease is a rare disease[1]. It draws 20 Wikipedia views per month (rare_disease category, ranking #220 of 627).[2]
Key Facts
- Dejerine–Sottas disease's instance of is recorded as rare disease[3].
- Dejerine–Sottas disease's instance of is recorded as class of disease[4].
- Joseph Jules Dejerine is named after Dejerine–Sottas disease[5].
- Jules Sottas is named after Dejerine–Sottas disease[6].
- Dejerine–Sottas disease's subclass of is recorded as Charcot–Marie–Tooth disease[7].
- Dejerine–Sottas disease's Commons category is recorded as Dejerine-Sottas disease[8].
- Dejerine–Sottas disease's OMIM ID is recorded as 145900[9].
- Dejerine–Sottas disease's ICD-9 ID is recorded as 356.0[10].
- Dejerine–Sottas disease's ICD-10 ID is recorded as G60.0[11].
- Dejerine–Sottas disease's DiseasesDB is recorded as 5821[12].
- Dejerine–Sottas disease's Orphanet ID is recorded as 64748[13].
- Dejerine–Sottas disease's health specialty is recorded as neurology[14].
- Dejerine–Sottas disease's genetic association is recorded as PRX[15].
- Dejerine–Sottas disease's genetic association is recorded as PMP22[16].
- Dejerine–Sottas disease's genetic association is recorded as MPZ[17].
- Dejerine–Sottas disease's BabelNet ID is recorded as 03410583n[18].
- Dejerine–Sottas disease's GARD rare disease ID is recorded as 9204[19].
- Dejerine–Sottas disease's Mondo ID is recorded as MONDO_0007790[20].
- Dejerine–Sottas disease's Microsoft Academic ID is recorded as 2780818367[21].
- Dejerine–Sottas disease's WikiProjectMed ID is recorded as Dejerine–Sottas disease[22].
- Dejerine–Sottas disease's UniProt disease ID is recorded as DI-00387[23].
Why It Matters
Dejerine–Sottas disease draws 20 Wikipedia views per month (rare_disease category, ranking #220 of 627).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[24] It is known by 9 alternative names across languages and contexts.[25]